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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 278248Generated: October 26, 2026

Triethylamine → 4-Piperidinemethanol, 1-benzoyl-

https://huagongshe.com/reaction/278248

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTriethylamineHCID 8471—
ReactantIsobutyl chloroformateHCID 62365—
Reactant1-Benzoylpiperidine-4-carboxylic acidHCID 78935—
ReactantSodium borohydrideHCID 4311764—
SolventWaterHCID 962—
SolventDimethylformamideHCID 6228—
SolventTetrahydrofuranHCID 8028—
Product4-Piperidinemethanol, 1-benzoyl-HCID 1026287099.2%

Reaction Conditions

Temperature0 °C

Reaction Steps

To a solution of 2 g of 1-benzoylisonipecotic acid (Step A) in 50 mL THF at 0° C. were added 1.47 g of triethylamine and 1.99 g of isobutyl chloroformate. The reaction was stirred for 1 h at 0° C. To a solution of 1.10 g of sodium borohydride in 30 mL DMF at 0° C. was slowly added the above THF mixture. The reaction was again stirred for 1 h at 0° C. Water (80 mL) was slowly added to the reaction and the mixture was extracted 5×80 mL ethyl acetate and the combined organic layers were dried over magnesium sulfate. The solvent was then evaporated under reduced pressure. The residue was purified by flash chromatography with 1:1 hexane : ethyl acetate followed by hexane : ethyl acetate: methanol, 50:50:5 to give 1.865 g of the title compound.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06358979B1
Source datasetuspto-grants-2002_03
ORD IDord-ac9768a399e142d29cfd64358aaa3407
Source noteuspto-grants-2002_03